Rituximab was used to treat recurrent IgG4-related hypophysitis with ophthalmopathy as the initial presentation: A case report and literature review

scientific article

Rituximab was used to treat recurrent IgG4-related hypophysitis with ophthalmopathy as the initial presentation: A case report and literature review is …
instance of (P31):
review articleQ7318358
case reportQ2782326
scholarly articleQ13442814

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P356DOI10.1097/MD.0000000000006934
P932PMC publication ID5478305
P698PubMed publication ID28614220

P2093author name stringJie Li
Qian Zhang
Jian Zhu
Yi-Ming Mu
Shi-Hui Wei
Wei-Jun Gu
P2860cites workThe prevalence of IgG4-related hypophysitis in 170 consecutive patients with hypopituitarism and/or central diabetes insipidus and review of the literatureQ26866028
International Consensus Guidance Statement on the Management and Treatment of IgG4-Related DiseaseQ27970302
Hypophysitis due to IgG4-related disease responding to treatment with azathioprine: an alternative to corticosteroid therapyQ30651194
Prednisolone markedly reduced serum IgG4 levels along with the improvement of pituitary mass and anterior pituitary function in a patient with IgG4-related infundibulo-hypophysitisQ30714403
Occurrence of IgG4-related hypophysitis lacking IgG4-bearing plasma cell infiltration during steroid therapyQ30791963
A case of suspected lymphocytic hypophysitis and organizing pneumonia during maintenance therapy for autoimmune pancreatitis associated with autoimmune thrombocytopeniaQ33371988
Long-term clinical course of IgG4-related systemic disease accompanied by hypophysitisQ33550042
Histologically confirmed isolated IgG4-related hypophysitis: two case reports in young women.Q34241475
IgG4-related hypophysitis: a new addition to the hypophysitis spectrum.Q35101828
Clinical course of IgG4-related hypophysitis presenting with focal seizure and relapsing lymphocytic hypophysitisQ35824920
Autoimmune hypophysitis.Q36000933
Hypophysitis presented as inflammatory pseudotumor in immunoglobulin G4-related systemic diseaseQ36978379
Optimising corticosteroid treatment for autoimmune pancreatitisQ36999326
IgG4-related sclerosing disease: a critical appraisal of an evolving clinicopathologic entityQ37781971
IgG4-related systemic disease in a Native American man.Q37866008
A case of IgG4-related hypophysitis without pituitary insufficiencyQ38091622
Clinical features of 10 patients with IgG4-related retroperitoneal fibrosisQ38121780
Inflammatory pseudotumors in multiple organs associated with elevated serum IgG4 level: recovery by only a small replacement dose of steroidQ40416847
IgG4-associated multifocal systemic fibrosis complicating sclerosing sialadenitis, hypophysitis, and retroperitoneal fibrosis, but lacking pancreatic involvement.Q40463357
Thickened Pituitary Stalk Associated with a Mass in the Sphenoidal Sinus: An Alarm to Suspect Hypophysitis by Immunoglobulin G4?Q41443579
IgG4-Related Disease without Overexpression of IgG4: Pathogenesis ImplicationsQ42278748
A Case of IgG4-Related Hypophysitis Presented with Hypopituitarism and Diabetes InsipidusQ42906513
Putative IgG4-related pituitary disease with hypopituitarism and/or diabetes insipidus accompanied with elevated serum levels of IgG4.Q43064024
Treatment of relapsing autoimmune pancreatitis with immunomodulators and rituximab: the Mayo Clinic experienceQ43472409
Standard steroid treatment for autoimmune pancreatitis.Q46034514
A case of IgG4-related multifocal fibrosclerosis complicated by central diabetes insipidusQ46584974
IgG4-related hypophysitis presenting as a pituitary adenoma with systemic diseaseQ48113939
Hypophysitis presenting with atypical rapid deterioration: with special reference to immunoglobulin G4-related disease-case report-.Q48368362
A case of Mikulicz's disease (IgG4-related plasmacytic disease) complicated by autoimmune hypophysitisQ48388498
[Two cases of IgG4-related systemic disease arising from urinary tract].Q50498642
[Clinicopathological features of neuropathy associated with IgG4-related disease].Q53620006
Amendment of the Japanese Consensus Guidelines for Autoimmune Pancreatitis, 2013 III. Treatment and prognosis of autoimmune pancreatitisQ60609861
High serum IgG4 concentrations in patients with sclerosing pancreatitisQ73583110
Autoimmune pancreatitisQ80147141
Multiple pseudotumors in IgG4-associated multifocal systemic fibrosisQ81104496
Serial changes of elevated serum IgG4 levels in IgG4-related systemic diseaseQ83232220
[A case of IgG4-related disease with deterioration in pulmonary and pituitary involvements during a 10-year clinical course of inflammatory pseudotumor]Q83480097
[Case report: IgG4-related hypophysitis presenting with secondary adrenal insufficiency and central diabetes insipidus in a type 1 diabetes patient]Q84232115
P275copyright licenseCreative Commons Attribution-NonCommercial-NoDerivs 4.0 InternationalQ24082749
P433issue24
P407language of work or nameEnglishQ1860
P921main subjectglobulinsQ321710
rituximabQ412323
monoclonal antibodyQ422248
blood proteinsQ425056
eye diseaseQ3041498
immunologic factorQ50349184
murine-derived monoclonal antibodiesQ68944048
P5008on focus list of Wikimedia projectScienceSourceQ55439927
P304page(s)e6934
P577publication date2017-06-01
P1433published inMedicineQ15716652
P1476titleRituximab was used to treat recurrent IgG4-related hypophysitis with ophthalmopathy as the initial presentation: A case report and literature review
P478volume96

Reverse relations

cites work (P2860)
Q47296234A case series of atypical features of patients with biopsy-proven isolated IgG4-related hypophysitis and normal serum IgG4 levels
Q92591462Clinical Characteristics of 76 Patients with IgG4-Related Hypophysitis: A Systematic Literature Review
Q64039689Disease heterogeneity in IgG4-related hypophysitis: report of two histopathologically proven cases and review of the literature
Q89310972Sustained clinical response after single course of rituximab as first-line monotherapy in adult-onset asthma and periocular xanthogranulomas syndrome associated with IgG4-related disease: A case report

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